2016
DOI: 10.1002/cssc.201600203
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Hydrogenation of Carbon Dioxide to Methane by Ruthenium Nanoparticles in Ionic Liquid

Abstract: The efficient transformation of carbon dioxide into fuels can be an excellent alternative to sequestration. In this work, we describe CO2 hydrogenation to methane in imidazolium-based ionic liquid media, using ruthenium nanoparticles prepared in situ as catalyst. The best yield of methane (69 %) was achieved using 0.24 mol % ruthenium catalyst (in [omim][NTf2 ], 1-octyl-3-methylimidazolium bistrifluoromethanesulfonylimide, at 40 bar of hydrogen pressure plus 40 bar of CO2 pressure, and at 150 °C.

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Cited by 43 publications
(26 citation statements)
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“…As a catalytic material, Ru has been extensively used to accelerate a range of reactions, including hydrogenation, CO oxidation, and ammonia decomposition . As mentioned previously, the phase diagram of bulk Ru suggests that its equilibrium phase under ambient conditions is hcp .…”
Section: Extension To Other Metals and Alloysmentioning
confidence: 93%
“…As a catalytic material, Ru has been extensively used to accelerate a range of reactions, including hydrogenation, CO oxidation, and ammonia decomposition . As mentioned previously, the phase diagram of bulk Ru suggests that its equilibrium phase under ambient conditions is hcp .…”
Section: Extension To Other Metals and Alloysmentioning
confidence: 93%
“…As a last example, Branco and coworkers described the hydrogenation of CO2 into methane using in situ formed IL-supported Ru NPs (Figure 26). 283 The nanocatalyst was prepared in situ Reprinted with permission from ref 283 . Copyright 2016 Wiley.…”
Section: Transformation Of Co2 Into Co Ch4 or C2+ Hydrocarbonsmentioning
confidence: 99%
“…Design of catalysts that can work effectively at lower temperature has received considerable attention. 29 Although many efforts have been made, the progress was restricted to several noble metal catalysts, especially at a temperature below 200 C. [30][31][32][33][34][35][36] Obviously, low temperature methanation of CO 2 over cheap metal catalysts is highly desirable. Herein we show that the amorphous Zrdoped Co-B-O catalyst can effectively accelerate the CO 2 methanation at above 140 C. Excellent activity was obtained at 180 C, which is comparable to or even higher than those of some noble metal catalysts (Table S1 †).…”
Section: Introductionmentioning
confidence: 99%